Class II ยท Moderate risk
Aripiprazole Tablets USP
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
National Drug Code
Is NDC 27241-0056-03 recalled?
Aripiprazole · 30 TABLET in 1 BOTTLE (27241-056-03)
Yes — this exact package was recalled
1 FDA recall names the code 27241-0056-03 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Aripiprazole
- Strength
- ARIPIPRAZOLE 30 mg/1
- Form
- Tablet · Oral
- Labeler
- Ajanta Pharma USA Inc.
- Type
- Human Prescription Drug
- Product code
- 27241-0056
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 27241-0097 Duloxetine 1
- 27241-0098 Duloxetine 1
- 27241-0099 Duloxetine 1
- 27241-0118 Fenofibrate 1
- 27241-0120 Fenofibrate 1
- 27241-0255 Fluphenazine hydrochloride 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.